FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MEDICOOL

K Number: K923643 · Decision Mar 31, 1993
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
92
Applicant Total
42
Review Days
253

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Basic Information

Device Name
MEDICOOL
K Number
K923643
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5720
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Micromedic Systems
Date Received
July 21, 1992
Decision Date
March 31, 1993
Product Code
ILO
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ILO Pack, Hot Or Cold, Water Circulating

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K870245 AUTOPAK TSH MONOCLONAL IRMA KIT
K862206 TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTER
K860813 MICROMEDIC HTSH MONOCLONAL IRMA KIT
K861262 MMS T3 UPTAKE
K861320 MMS T4 RIA KIT
K853127 MICROMEDIC COMBOSTAT B B12/FOLATE(BOIL)
Search all 42 clearances from Micromedic Systems →